Variant report

Variant	rs73535776
Chromosome Location	chr15:92847651-92847652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs57816248	0.83[AMR][1000 genomes]
rs58194078	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59058379	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60165283	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7169408	0.83[AMR][1000 genomes]
rs73533682	0.83[AMR][1000 genomes]
rs73535760	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73535773	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74030508	0.83[AMR][1000 genomes]
rs8023418	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92838400-92847800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:92847200-92847800	Enhancers	Primary hematopoietic stem cells	blood
3	chr15:92847200-92848000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr15:92847200-92848200	Enhancers	Fetal Heart	heart
5	chr15:92847200-92848800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:92847200-92850000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr15:92847200-92850200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr15:92847200-92850600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr15:92847400-92848000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr15:92847400-92850000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:92847400-92850400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:92847400-92850400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr15:92847600-92847800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
14	chr15:92847600-92848600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr15:92847600-92848800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr15:92847600-92850400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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